1 of 7 Epi4K: Gene discovery in 4,000 epilepsy genomes - Administrative Core
1 of 7 Epi4K: Gene discovery in 4,000 epilepsy genomes - Administrative Core
批准号:
8338464
负责人:
David B. Goldstein
金额:
$15.94万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-09-30 至 2016-07-30
关键词:
AffectBioinformaticsBiometryClinical InformaticsCollaborationsCommunicationDNA Sequencing FacilityDataDiagnosticDiseaseElectronicsEpilepsyFamilyFamily memberGenesGeneticGenomeGoalsHousingHumanHuman GenomeIndividualLeadershipLifeMissionNational Institute of Neurological Disorders and StrokePathway interactionsPatientsPersonal SatisfactionPhenotypePopulationPrincipal InvestigatorProtocols documentationPublicationsRecurrenceReportingResearchResearch PersonnelRiskTeleconferencesUniversitiesVariantWorkbasecareer developmentdata sharingethical legal social implicationgene discoveryimprovedmedical schoolsmeetingsmembernervous system disorderprognostic
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The primary goal of the Epi4K Center Without Walls is to increase understanding of the genetic basis of human epilepsy in order to improve the well-being of patients and family members living with these disorders. This improvement will come in the form of better diagnostics, treatments and cures. To accomplish this goal, Epi4K aims to analyze the genomes of a large number of well-phenotyped epilepsy patients and families collected by investigators from several major research groups. The specific goals of this project (1 of 7 - Administrative Core) are to provide overall leadership to the Center, specifically regarding the Center's charter, universal protocols, plans for data sharing, internal and external communications, and tracking of scientific progress of all cores and projects within the Center.
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An integrated and diverse genomic medicine program for undiagnosed diseases
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资助金额:$79.94万
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资助金额:$137.93万
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依托单位:
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财政年份:2013
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依托单位:
Identifying de novo mutations causing OCD in trios by whole exome sequencing
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资助金额:$79.18万
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依托单位:
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资助金额:$12.97万
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财政年份:2013
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依托单位:
Identifying de novo mutations causing OCD in trios by whole exome sequencing
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依托单位:
Identifying de novo mutations causing OCD in trios by whole exome sequencing
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依托单位:
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项目类别:
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项目类别:
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依托单位:
海外基金